Canonical Allele Identifier: CA349488672

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179456705G>T (hg19) ; chr2:g.178591978G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178591978G>T , CM000664.2:g.178591978G>T	GRCh38
NC_000002.11:g.179456705G>T , CM000664.1:g.179456705G>T	GRCh37
NC_000002.10:g.179164951G>T	NCBI36
NG_011618.3:g.243825C>A , LRG_391:g.243825C>A
NG_051363.1:g.74152G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.52222C>A (TTN)	ENSP00000343764.6:p.His17408Asn
ENST00000342175.11:c.33307C>A (TTN)	ENSP00000340554.6:p.His11103Asn
ENST00000359218.10:c.33106C>A (TTN)	ENSP00000352154.5:p.His11036Asn
ENST00000342175.10:c.33307C>A (TTN)	ENSP00000340554.6:p.His11103Asn
ENST00000342992.10:c.52222C>A (TTN)	ENSP00000343764.6:p.His17408Asn
ENST00000359218.9:c.33106C>A (TTN)	ENSP00000352154.5:p.His11036Asn
ENST00000460472.6:c.32731C>A (TTN)	ENSP00000434586.1:p.His10911Asn
ENST00000589042.5:c.59926C>A (TTN) MANE Select	ENSP00000467141.1:p.His19976Asn
ENST00000591111.5:c.55003C>A (TTN)	ENSP00000465570.1:p.His18335Asn
ENST00000615779.4:c.55003C>A (TTN)	ENSP00000483597.1:p.His18335Asn
NM_001256850.1:c.55003C>A (TTN)	NP_001243779.1:p.His18335Asn
NM_001267550.2:c.59926C>A (TTN) MANE Select	NP_001254479.2:p.His19976Asn
NM_003319.4:c.32731C>A (TTN)	NP_003310.4:p.His10911Asn
NM_133378.4:c.52222C>A (TTN)	NP_596869.4:p.His17408Asn
NM_133432.3:c.33106C>A (TTN)	NP_597676.3:p.His11036Asn
NM_133437.4:c.33307C>A (TTN)	NP_597681.4:p.His11103Asn
NR_038271.1:n.597-5618G>T (TTN-AS1)
NR_038272.1:n.3364+664G>T (TTN-AS1)
XM_011511729.1:c.59023C>A (TTN)	XP_011510031.1:p.His19675Asn
XM_011511730.1:c.32917C>A (TTN)	XP_011510032.1:p.His10973Asn
XM_011511731.1:c.32776C>A (TTN)	XP_011510033.1:p.His10926Asn
XM_017004819.1:c.58819C>A (TTN)	XP_016860308.1:p.His19607Asn
XM_017004820.1:c.54217C>A (TTN)	XP_016860309.1:p.His18073Asn
XM_017004821.1:c.54214C>A (TTN)	XP_016860310.1:p.His18072Asn
XM_017004822.1:c.51256C>A (TTN)	XP_016860311.1:p.His17086Asn
XM_017004823.1:c.32872C>A (TTN)	XP_016860312.1:p.His10958Asn
XM_024453094.1:c.54367C>A (TTN)	XP_024308862.1:p.His18123Asn
XM_024453095.1:c.54364C>A (TTN)	XP_024308863.1:p.His18122Asn
XM_024453096.1:c.53797C>A (TTN)	XP_024308864.1:p.His17933Asn
XM_024453097.1:c.51139C>A (TTN)	XP_024308865.1:p.His17047Asn
XM_024453098.1:c.51058C>A (TTN)	XP_024308866.1:p.His17020Asn
XM_024453099.1:c.32821C>A (TTN)	XP_024308867.1:p.His10941Asn
XM_024453100.1:c.22675C>A (TTN)	XP_024308868.1:p.His7559Asn